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| Title : EPHX1 mutations cause a lipoatrophic diabetes syndrome due to impaired epoxide hydrolysis and increased cellular senescence - Gautheron_2021_Elife_10_ |
| Author(s) : Gautheron J , Morisseau C , Chung WK , Zammouri J , Auclair M , Baujat G , Capel E , Moulin C , Wang Y , Yang J , Hammock BD , Cerame B , Phan F , Feve B , Vigouroux C , Andreelli F , Jeru I |
| Ref : Elife , 10 : , 2021 |
| Abstract : Gautheron_2021_Elife_10_ |
| ESTHER : Gautheron_2021_Elife_10_ |
| PubMedSearch : Gautheron_2021_Elife_10_ |
| PubMedID: 34342583 |
| Gene_locus related to this paper: human-EPHX1 |
| Title : Lipodystrophic syndromes: From diagnosis to treatment - Sollier_2020_Ann.Endocrinol.(Paris)_81_51 |
| Author(s) : Sollier C , Vatier C , Capel E , Lascols O , Auclair M , Janmaat S , Feve B , Jeru I , Vigouroux C |
| Ref : Ann Endocrinol (Paris) , 81 :51 , 2020 |
| Abstract : Sollier_2020_Ann.Endocrinol.(Paris)_81_51 |
| ESTHER : Sollier_2020_Ann.Endocrinol.(Paris)_81_51 |
| PubMedSearch : Sollier_2020_Ann.Endocrinol.(Paris)_81_51 |
| PubMedID: 31982105 |